Cargando…

Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function

Phagocytosis is a fundamental cellular process that is pivotal for immunity as it coordinates microbial killing, innate immune activation and antigen presentation. An essential step in this process is phagosome acidification, which regulates a number of functions of these organelles that allow them...

Descripción completa

Detalles Bibliográficos
Autores principales: Sokolovska, Anna, Becker, Christine E., Eddie Ip, WK, Rathinam, Vijay A.K., Brudner, Matthew, Paquette, Nicholas, Tanne, Antoine, Vanaja, Sivapriya K., Moore, Kathryn J., Fitzgerald, Katherine A., Lacy-Hulbert, Adam, Stuart, Lynda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708594/
https://www.ncbi.nlm.nih.gov/pubmed/23644505
http://dx.doi.org/10.1038/ni.2595
_version_ 1782276637093527552
author Sokolovska, Anna
Becker, Christine E.
Eddie Ip, WK
Rathinam, Vijay A.K.
Brudner, Matthew
Paquette, Nicholas
Tanne, Antoine
Vanaja, Sivapriya K.
Moore, Kathryn J.
Fitzgerald, Katherine A.
Lacy-Hulbert, Adam
Stuart, Lynda M.
author_facet Sokolovska, Anna
Becker, Christine E.
Eddie Ip, WK
Rathinam, Vijay A.K.
Brudner, Matthew
Paquette, Nicholas
Tanne, Antoine
Vanaja, Sivapriya K.
Moore, Kathryn J.
Fitzgerald, Katherine A.
Lacy-Hulbert, Adam
Stuart, Lynda M.
author_sort Sokolovska, Anna
collection PubMed
description Phagocytosis is a fundamental cellular process that is pivotal for immunity as it coordinates microbial killing, innate immune activation and antigen presentation. An essential step in this process is phagosome acidification, which regulates a number of functions of these organelles that allow them to participate in processes essential to both innate and adaptive immunity. Here we report that acidification of phagosomes containing Gram-positive bacteria is regulated by the NLRP3-inflammasome and caspase-1. Active caspase-1 accumulates on phagosomes and acts locally to control the pH by modulating buffering by the NADPH oxidase NOX2. These data provide insight into a mechanism by which innate immune signals can modify cellular defenses and establish a new function for the NLRP3-inflammasome and caspase-1 in host defense.
format Online
Article
Text
id pubmed-3708594
institution National Center for Biotechnology Information
language English
publishDate 2013
record_format MEDLINE/PubMed
spelling pubmed-37085942013-12-01 Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function Sokolovska, Anna Becker, Christine E. Eddie Ip, WK Rathinam, Vijay A.K. Brudner, Matthew Paquette, Nicholas Tanne, Antoine Vanaja, Sivapriya K. Moore, Kathryn J. Fitzgerald, Katherine A. Lacy-Hulbert, Adam Stuart, Lynda M. Nat Immunol Article Phagocytosis is a fundamental cellular process that is pivotal for immunity as it coordinates microbial killing, innate immune activation and antigen presentation. An essential step in this process is phagosome acidification, which regulates a number of functions of these organelles that allow them to participate in processes essential to both innate and adaptive immunity. Here we report that acidification of phagosomes containing Gram-positive bacteria is regulated by the NLRP3-inflammasome and caspase-1. Active caspase-1 accumulates on phagosomes and acts locally to control the pH by modulating buffering by the NADPH oxidase NOX2. These data provide insight into a mechanism by which innate immune signals can modify cellular defenses and establish a new function for the NLRP3-inflammasome and caspase-1 in host defense. 2013-05-05 2013-06 /pmc/articles/PMC3708594/ /pubmed/23644505 http://dx.doi.org/10.1038/ni.2595 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Sokolovska, Anna
Becker, Christine E.
Eddie Ip, WK
Rathinam, Vijay A.K.
Brudner, Matthew
Paquette, Nicholas
Tanne, Antoine
Vanaja, Sivapriya K.
Moore, Kathryn J.
Fitzgerald, Katherine A.
Lacy-Hulbert, Adam
Stuart, Lynda M.
Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function
title Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function
title_full Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function
title_fullStr Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function
title_full_unstemmed Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function
title_short Activation of caspase-1 by the NLRP3 inflammasome regulates the NADPH oxidase NOX2 to control phagosome function
title_sort activation of caspase-1 by the nlrp3 inflammasome regulates the nadph oxidase nox2 to control phagosome function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708594/
https://www.ncbi.nlm.nih.gov/pubmed/23644505
http://dx.doi.org/10.1038/ni.2595
work_keys_str_mv AT sokolovskaanna activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT beckerchristinee activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT eddieipwk activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT rathinamvijayak activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT brudnermatthew activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT paquettenicholas activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT tanneantoine activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT vanajasivapriyak activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT moorekathrynj activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT fitzgeraldkatherinea activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT lacyhulbertadam activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction
AT stuartlyndam activationofcaspase1bythenlrp3inflammasomeregulatesthenadphoxidasenox2tocontrolphagosomefunction